ABSTRACT
The diagnostic criteria for gestational diabetes mellitus (GDM), a transient hyperglycemic state during pregnancy, has varied remarkably over time, resulting in a diversity of prevalence rates. The aim of this systematic literature review was to provide estimates of prevalence rates of GDM in Brazil according to different diagnostic criteria. We identified, reviewed, and extracted data from the scientific literature on studies estimating the prevalence of diabetes in pregnant women living in Brazil. The databases searched were PubMed, LILACS, SciELO, Embase, Web of Science, and Cochrane Library. We grouped studies by the source of information assessing GDM, patients’ age, and criteria used to diagnose GDM. When three or more studies were available in a group, we calculated the pooled prevalence. The Joanna Briggs Institute (JBI) appraisal tool was used to assess the risk of bias. The data were reported according to the 2020 PRISMA recommendations. The study protocol was registered in PROSPERO. We identified 1,328 records and selected 21 studies involving 122,635 pregnant women. Studies in adults only, with primary data and laboratory measurements, and using the IADPSG criteria (n = 3) had a GDM prevalence of 18.0% (95% confidence interval [CI]: 16.0-20.1%) and included 6,243 participants. Estimates of self-reported GDM (n = 3; 10,136 participants of all ages) had a pooled GDM prevalence of 2.1% (95% CI: 1.5-5.2%), with high heterogeneity (I2 = 85.0%, p < 0.01). Studies including adolescents had consistently low prevalences. The prevalence of GDM in Brazil varied, was greater when the IADPSG criteria were applied, and depended on the methods used to obtain the GDM information and the age structure of the sample.
Keywords
Gestational diabetes; Brazil; prevalence; epidemiology
INTRODUCTION
Gestational diabetes mellitus (GDM), a transient hyperglycemic state diagnosed in pregnancy, is associated with adverse maternal and fetal outcomes (11 Ye W, Luo C, Huang J, Li C, Liu Z, Liu F. Gestational diabetes mellitus and adverse pregnancy outcomes: systematic review and meta-analysis. BMJ. 2022;377:e067946. DOI: 10.1136/bmj-2021-067946
https://doi.org/10.1136/bmj-2021-067946...
). Although the concept of GDM is generally consensual, the diagnostic criteria for GDM have experienced marked heterogeneity over time, resulting in diverse prevalence rates, as attested by systematic reviews across different countries, regions, and even globally (22 Behboudi-Gandevani S, Amiri M, Bidhendi Yarandi R, Ramezani Tehrani F. The impact of diagnostic criteria for gestational diabetes on its prevalence: a systematic review and meta-analysis. Diabetol Metab Syndr. 2019;11(1):11. DOI: 10.1186/s13098-019-0406-1
https://doi.org/10.1186/s13098-019-0406-...
–44 Muche AA, Olayemi OO, Gete YK. Prevalence and determinants of gestational diabetes mellitus in Africa based on the updated international diagnostic criteria: a systematic review and meta-analysis. Arch Public Health. 2019;77(1):36. DOI: 10.1186/s13690-019-0362-0
https://doi.org/10.1186/s13690-019-0362-...
).
In Brazil, routine detection of GDM was incipient before the implementation of the national health unified system (Sistema Único de Saúde [SUS]). Screening for GDM was generally restricted to university centers and usually followed the guidelines of the American Diabetes Association (ADA) based on pregnancy-specific criteria. These guidelines were derived from a series of studies conducted methodically by O’Sullivan's group (55 O'Sullivan JB. Establishing criteria for gestational diabetes. Diabetes Care. 1980;3(3):437-9. DOI: 10.2337/diacare.3.3.437
https://doi.org/10.2337/diacare.3.3.437...
). The ADA position was reiterated in 1979 by the National Diabetes Data Group (NDDG), when the diagnostic criteria for diabetes and other categories of glucose intolerance were defined (66 National Diabetes Data Group. Classification and diagnosis of diabetes mellitus and other categories of glucose intolerance. Diabetes. 1979;28(12):1039-57. DOI: 10.2337/diab.28.12.1039
https://doi.org/10.2337/diab.28.12.1039...
). The recommended diagnostic procedure for GDM was based on a two-stage screening in which the patients initially underwent a 50-g glucose challenge, and those with a positive result underwent a 100-g oral glucose tolerance test (OGTT) with samples collected at fasting and at 1, 2, and 3 hours. The diagnosis of GDM was defined as the presence of at least two abnormal plasma glucose results. While agreeing with most NDDG recommendations, a World Health Organization (WHO) panel in 1980 defined GDM using the same criteria applied outside pregnancy for impaired glucose tolerance (77 World Health Organization. WHO Expert Committee on Diabetes Mellitus [meeting held in Geneva from 25 September to 1 October 1979]: second report. Geneva: WHO; 1980.), without specifying a cutoff value for fasting glucose levels.
Confronted with this diagnostic controversy, the Brazilian Ministry of Health conducted a national study – the Brazilian Study of Gestational Diabetes (88 Schmidt MI, Duncan BB, Reichelt AJ, Branchtein L, Matos MC, Costa e Forti A, et al. Gestational diabetes mellitus diagnosed with a 2-h 75-g oral glucose tolerance test and adverse pregnancy outcomes. Diabetes Care. United States; 2001;24(7):1151-5. DOI: 10.2337/diacare.24.7.1151
https://doi.org/10.2337/diacare.24.7.115...
). In the study, the protocol for GDM diagnosis involved a 2-hour 75-g OGTT, with samples collected at fasting and at 1 and 2 hours. During a workshop, the panel recommended adopting a two-stage screening, in which the patient would first undergo measurement of fasting plasma glucose level and, if elevated, a 2-hour 75-g OGTT, defining GDM according to the same criteria established for impaired glucose tolerance outside pregnancy (99 Schmidt MI, Reichelt AJ. Consenso sobre diabetes gestacional e diabetes pré-gestacional. Arq Bras Endocrinol Metab. 1999;43(1):14-20. DOI: 10.1590/S0004-27301999000100005
https://doi.org/10.1590/S0004-2730199900...
). While adopting the same criteria established for impaired fasting glucose outside pregnancy (≥100 mg/dL or 110 mg/dL) (1010 The Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Diabetes Care. 1997;20(7):1183-97. DOI: 10.2337/diacare.20.7.1183
https://doi.org/10.2337/diacare.20.7.118...
), the panel also considered including this category in the definition of GDM (99 Schmidt MI, Reichelt AJ. Consenso sobre diabetes gestacional e diabetes pré-gestacional. Arq Bras Endocrinol Metab. 1999;43(1):14-20. DOI: 10.1590/S0004-27301999000100005
https://doi.org/10.1590/S0004-2730199900...
).
In 2008, new data on GDM emerged with the publication of the study Hyperglycemia and Adverse Pregnancy Outcomes (HAPO) (1111 The HAPO Study Cooperative Research Group. Hyperglycemia and adverse pregnancy outcomes. N Engl J Med. 2008;358(19):1991-2002. DOI: 10.1056/NEJMoa0707943
https://doi.org/10.1056/NEJMoa0707943...
), which involved more than 23,000 women across nine countries. The study's results compelled a committee of experts – The International Association of the Diabetes and Pregnancy Study Groups (IADPSG) – to develop and validate the diagnostic criteria for GDM based on adverse pregnancy outcomes. The procedures and criteria proposed were agreed upon during international meetings and were published in 2010 (1212 International Association of Diabetes and Pregnancy Study Groups Consensus Panel. International Association of Diabetes and Pregnancy Study Groups recommendations on the diagnosis and classification of hyperglycemia in pregnancy. Diabetes Care. 2010;33(3):676-82. DOI: 10.2337/dc09-1848
https://doi.org/10.2337/dc09-1848...
). The main recommendation from the committee was to adopt universal screening with a 2-hour 75-g OGTT (fasting and 1 and 2 hours) and consider the diagnosis of GDM when one or more values were abnormal. These criteria have been increasingly adopted (1313 Hod M, Kapur A, Sacks DA, Hadar E, Agarwal M, Di Renzo GC, et al. The International Federation of Gynecology and Obstetrics (FIGO) Initiative on gestational diabetes mellitus: A pragmatic guide for diagnosis, management, and care. Int J Gynaecol Obstet. 2015;131 Suppl 3:S173-211. DOI: 10.1016/S0020-7292(15)30033-3
https://doi.org/10.1016/S0020-7292(15)30...
–1515 World Health Organization. Diagnostic criteria and classification of hyperglycaemia first detected in pregnancy. Geneva: WHO; 2013.), but the controversy around them persists.
In 2014 in the United Kingdom, the National Institute for Health and Care Excellence (NICE) (1616 National Institute for Health and Care Excellence. Diabetes in pregnancy: management from preconception to the postnatal period. London: NICE; 2020.) proposed a two-stage screening for women at high risk for GDM based on a 2-hour 75-g OGTT. Although their definition of GDM included the cutoff value considered for impaired glucose tolerance outside pregnancy (as recommended by the 1979 WHO panel), the NICE recommendations also incorporated the cutoff value of 100 mg/dL for fasting plasma glucose.
In the United States, a consensus from a 2012 National Institutes of Health (NIH) conference recommended maintaining the two-stage screening procedure based on O’Sullivan's criteria (with Carpenter and Coustan corrections) (55 O'Sullivan JB. Establishing criteria for gestational diabetes. Diabetes Care. 1980;3(3):437-9. DOI: 10.2337/diacare.3.3.437
https://doi.org/10.2337/diacare.3.3.437...
). The ADA maintained this recommendation but also included the option of universal screening based on IADPSG procedures and criteria (1717 ElSayed NA, Aleppo G, Aroda VR, Bannuru RR, Brown FM, Bruemmer D, et al. 2. Classification and Diagnosis of Diabetes: Standards of Care in Diabetes—2023. Diabetes Care. 2023;46(Supplement_1):S19-40. DOI: 10.2337/dc23-S002
https://doi.org/10.2337/dc23-S002...
).
The debate continues. A comparison of these two screening criteria – IADPSG and Carpenter-Coustan – showed a substantial increase in GDM prevalence with the IADPSG criteria but did not detect improvement in pregnancy outcomes (55 O'Sullivan JB. Establishing criteria for gestational diabetes. Diabetes Care. 1980;3(3):437-9. DOI: 10.2337/diacare.3.3.437
https://doi.org/10.2337/diacare.3.3.437...
,66 National Diabetes Data Group. Classification and diagnosis of diabetes mellitus and other categories of glucose intolerance. Diabetes. 1979;28(12):1039-57. DOI: 10.2337/diab.28.12.1039
https://doi.org/10.2337/diab.28.12.1039...
).
In Brazil, a 2016 consensus panel proposed two strategies for GDM screening and diagnosis, to be chosen according to the financial viability and technical resources in different regions of the country (1818 Organização Pan-Americana da Saúde. Rastreamento e diagnóstico de diabetes mellitus gestacional no Brasil. Brasília: OPAS; 2017.).
Given the diversity of diagnostic criteria that emerged over the last decades and the long experience in GDM screening in Brazil, we aimed to conduct a systematic review of the pertinent literature on the prevalence of GDM in the country, establishing no limit for the year of publication.
MATERIALS AND METHODS
The study protocol was registered in PROSPERO (February 14, 2022) under the title “Prevalence of gestational diabetes in Brazil: a systematic review” and can be accessed online using the record ID CRD42022300767 (https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=300767).
We used the following search strategy to conduct the systematic literature review of original studies on the prevalence of GDM in pregnant women in Brazil. First, we searched the PubMed database (US National Library of Medicine, NIH). Then, we replicated the search in other databases, specifically, LILACS (Literatura Latino-Americana e do Caribe em Ciências da Saúde), SciELO, Embase, Web of Science, and Cochrane Library. For the search, we included free text words and indexed vocabulary (DeCS Health Science Descriptors) for articles published in Portuguese and used Medical Subject Headings (MeSH) terms for the Medline/PubMed search. The initial terms were: (prevalence OR prevalence [MeSH Terms] OR survey OR epidemiology OR incidence) AND (diabetes mellitus [MeSH Terms] OR diabetes OR hyperglycemia) AND (pregnant* OR gestation* OR gravid*) AND (brasil OR brazil). The complete PubMed search strategy is available in the Supplementary Material.
Selection of studies
The search was limited to studies in humans, without restriction of publication language or year, from the oldest records available until November 2021. A library with all the records found in the search was created by the researcher LFA using the software Zotero (https://www.zotero.org/). After removing duplicates, we uploaded the file into the software Rayyan to organize the references and share the file among the researchers for study selection and data extraction.
Using the list of references, two researchers (MLSC, SARE) independently screened the studies by reading the titles and abstracts using the following inclusion criteria (PICO framework): (A) Population: general population of pregnant women living in Brazil, regardless of gestational age, sample size, or study setting; (B) I: diagnostic methods applied, including fasting plasma glucose (FPG), OGTT, glycated hemoglobin (HbA1c), previous self-reported diagnosis of GDM, or direct evaluation of medical record; (C) Outcome measure: prevalence of GDM diagnosed according to screening methods; (D) Study design: observational study estimating prevalence data. Since our study aimed to describe the population's GDM prevalence, we did not include the “C” (comparison or control) from the PICO acronym. We excluded studies conducted on groups with specific pathologies, review articles, editorials, case-control studies, and studies with incomplete data estimating prevalence. In cases of disagreement, we consulted the full-text papers with the help of a third researcher experienced in the field (BPMI). In doubtful cases, the record was considered eligible for full-text reading.
After the initial screening, the full text was read independently by two researchers (MLSC, SARE) and later revised by two other researchers (BPMI, CS). During the full-text reading, we excluded studies that did not meet all the eligibility criteria or those that selected women at high risk for GDM (due to lifestyle and medical factors) or from high-risk prenatal centers, as detailed in Figure 1.
Data extraction
The primary outcome for analysis was the prevalence of GDM in pregnant women living in Brazil, regardless of gestational age. We extracted the data using a standard form built into a Google Spreadsheet containing items of interest to the review for use by the reviewers after initial training (BPMI, MLSC, SARE). The data, compiled for each study, included the following: first author, year of publication, study or cohort name (when available), location (city, state, region), year of data collection, method used for sample selection, study design, sample size, method used to define the outcome (self-reporting, medical record, or primary laboratory data), diagnostic criteria used to analyze the medical record or laboratory data, number of cases diagnosed with GDM, and prevalence rate reported in each study. If more than one study used the same database or population, we included only the study with the largest sample size or complete information. In case of disagreement, we consulted a senior researcher (MIS).
The data were reported according to the 2020 Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) recommendations. The inclusion/exclusion process is described in Figure 1.
Methodological quality appraisal
The researchers BPMI, MLSC, and SARE assessed the studies’ quality and risk of bias using the Joanna Briggs Institute (JBI) appraisal tool checklist for prevalence studies. For the evaluation, we considered the appropriateness of the sample frame and recruitment of participants, adequacy of the sample size, description of the subjects and settings, validity of the identification method, standardization of the condition measured, adequacy of the statistical analysis, and rate of responses. We adapted the evaluation of these parameters for the specific setting of our GDM question, considering also scales used in similar systematic reviews, such as those used by Hoy and cols. (1919 Hoy D, Brooks P, Woolf A, Blyth F, March L, Bain C, et al. Assessing risk of bias in prevalence studies: modification of an existing tool and evidence of interrater agreement. J Clin Epidemiol. 2012;65(9):934-9. DOI: 10.1016/j.jclinepi.2011.11.014
https://doi.org/10.1016/j.jclinepi.2011....
) and Muche and cols. (44 Muche AA, Olayemi OO, Gete YK. Prevalence and determinants of gestational diabetes mellitus in Africa based on the updated international diagnostic criteria: a systematic review and meta-analysis. Arch Public Health. 2019;77(1):36. DOI: 10.1186/s13690-019-0362-0
https://doi.org/10.1186/s13690-019-0362-...
). We adapted the criteria of representativeness to the setting of studies of GDM, usually conducted within the health services. We considered a sample to be drawn from the general population of pregnant women when the source covered the majority of the population, such as population registries, general practice registries, or registries of clinics for pregnant women.
We considered the sample size adequate when it was calculated a priori. We considered the description of the subjects and settings adequate if the participants’ mean age and body mass index (BMI) were available. We considered having a low risk of bias those studies that used methods to identify GDM based on a laboratory test (e.g., OGTT, FPG, HbA1c) or laboratory data from medical records. We considered other methods (such as those from medical records with no specification of the test used or self-reported GDM) as having a high or uncertain risk of bias. The identification method was considered standardized when it used the same approach for data collection for all patients (a unique criterion) and training of the researchers on data extraction for each study. We considered the response rate adequate when ≥75% (44 Muche AA, Olayemi OO, Gete YK. Prevalence and determinants of gestational diabetes mellitus in Africa based on the updated international diagnostic criteria: a systematic review and meta-analysis. Arch Public Health. 2019;77(1):36. DOI: 10.1186/s13690-019-0362-0
https://doi.org/10.1186/s13690-019-0362-...
,1919 Hoy D, Brooks P, Woolf A, Blyth F, March L, Bain C, et al. Assessing risk of bias in prevalence studies: modification of an existing tool and evidence of interrater agreement. J Clin Epidemiol. 2012;65(9):934-9. DOI: 10.1016/j.jclinepi.2011.11.014
https://doi.org/10.1016/j.jclinepi.2011....
), considering the study's total target population when described. We considered the statistical analysis adequate when the study provided values for the total sample size (denominator) and total number of GDM cases (numerator) to allow for the estimation of prevalence. When the information provided was insufficient, we agreed to grade that item as unclear (uncertain).
Analysis
We initially grouped the studies according to the methods they used to identify GDM into (A) primary data and laboratory measurements, (B) medical records, and (C) self-reporting. If individual studies reported multiple prevalence rates based on different diagnostic criteria, we included each specific finding for the initial grouping. Then, based on the number of events and sample size obtained for each study, we calculated the pooled prevalence using a random effects model for each subgroup whenever three or more studies were available. We chose the random effects model to combine studies due to the nature of observational studies and the certainty of heterogeneity among them, even between studies with the same diagnostic criteria. We built forest plots to visualize the extent of the heterogeneity between studies. We considered the presence of heterogeneity when I2 was ≥50% and the Cochran's Q test and its respective p value was < 0.05. We conducted analyses using R language in RStudio (RStudio PBC, Boston, MA, USA) and the packages meta and metafor.
RESULTS
Description of the studies included in the review
The database search identified 1,328 records from January 1, 1965 (when the first document was available) to November 30, 2021. After removal of duplicates (n = 438) and exclusions by title and abstract (n = 838), 52 studies were considered eligible for full-text reading. Of these, 29 were excluded as they duplicated reports of studies already included (n = 16) or had a different outcome (n = 4), population (n = 7), or study design (n = 2). We also excluded records based on conference proceedings (n = 2) and those without full text accessible online (n = 1). One study published recently was added by an expert (BPMI) due to its potential relevance. Altogether, we extracted results from 21 studies. The PRISMA flowchart of study identification is presented in Figure 1.
We evaluated the 21 studies according to the method they used to assess the occurrence of GDM, i.e., primary data with laboratory measurements (FPG, OGTT, or a combination of both; n = 10) (88 Schmidt MI, Duncan BB, Reichelt AJ, Branchtein L, Matos MC, Costa e Forti A, et al. Gestational diabetes mellitus diagnosed with a 2-h 75-g oral glucose tolerance test and adverse pregnancy outcomes. Diabetes Care. United States; 2001;24(7):1151-5. DOI: 10.2337/diacare.24.7.1151
https://doi.org/10.2337/diacare.24.7.115...
,2020 Nicolosi BF, Souza RT, Mayrink J, Feitosa FE, Rocha Filho EA, Leite DF, et al. Incidence and risk factors for hyperglycemia in pregnancy among nulliparous women: A Brazilian multicenter cohort study. PLoS One. 2020;15(5):e0232664. DOI: 10.1371/journal.pone.0232664
https://doi.org/10.1371/journal.pone.023...
–2828 Alves JG, Souza ASR, Figueiroa JN, de Araújo CAL, Guimarães A, Ray JG. Visceral adipose tissue depth in early pregnancy and gestational diabetes mellitus - a cohort study. Sci Rep. 2020;10(1):2032. DOI: 10.1038/s41598-020-59065-5
https://doi.org/10.1038/s41598-020-59065...
), self-reported GDM diagnosis (n = 3) (2929 Dode MAS de O, Santos I da S dos. Fatores de risco para diabetes mellitus gestacional na coorte de nascimentos de Pelotas, Rio Grande do Sul, Brasil, 2004. Cad Saúde Pública. 2009;25(5):1141-52. DOI: 10.1590/S0102-311X2009000500021
https://doi.org/10.1590/S0102-311X200900...
–3131 Dode MAS de O, Santos IS. Validade do auto-relato de diabete mellitus gestacional no pós-parto imediato. Cad Saúde Pública. 2009;25(2):251-8. DOI: 10.1590/S0102-311X2009000200003
https://doi.org/10.1590/S0102-311X200900...
), self-reported diabetes during pregnancy without specifying the type of diabetes (n = 1) (3232 Souza CM, Malta DC, Iser BPM. Diabetes gestacional autorreferido – uma análise da Pesquisa Nacional de Saúde. Cad Saúde Coletiva. 2022; in press.), medical records with previous diagnostic tests (such as a medical chart or prenatal card; n = 6) (3131 Dode MAS de O, Santos IS. Validade do auto-relato de diabete mellitus gestacional no pós-parto imediato. Cad Saúde Pública. 2009;25(2):251-8. DOI: 10.1590/S0102-311X2009000200003
https://doi.org/10.1590/S0102-311X200900...
,3333 Brandao T, Padilha P de C, Nogueira da Gama SG, Leal M do C, Pimenta da Silva Araujo RG, de Barros DC, et al. Gestational weight gain and adverse maternal outcomes in Brazilian women according to body mass index categories: An analysis of data from the Birth in Brazil survey. Clin Nutr ESPEN. 2020;37:114-20. DOI: 10.1016/j.clnesp.2020.03.009
https://doi.org/10.1016/j.clnesp.2020.03...
‣3737 Oliveira ACM de, Graciliano NG. Síndrome hipertensiva da gravidez e diabetes mellitus gestacional em uma maternidade pública de uma capital do Nordeste brasileiro, 2013: prevalência e fatores associados. Epidemiol Serv Saúde. 2015;24(3):441-51. DOI: 10.5123/S1679-49742015000300010
https://doi.org/10.5123/S1679-4974201500...
), and data collected using other systems (including the International Classification of Diseases [ICD]), for which specific criteria could not be identified (n = 2) (3838 Teixeira CR de S, Franco LJ, Monteiro RA, Granado F. Diabetes nos partos hospitalares em sistemas de saúde público e privado. Rev Saúde Pública. 2013;47(3):460-9. DOI: 10.1590/s0034-8910.2013047003687
https://doi.org/10.1590/s0034-8910.20130...
,3939 Silva de Morais N, Ayres Saraiva D, Corcino C, Berbara T, Schtscherbyna A, Moreira K, et al. Consequences of Iodine Deficiency and Excess in Pregnancy and Neonatal Outcomes: A Prospective Cohort Study in Rio de Janeiro, Brazil. Thyroid. United States; 2020;30(12):1792-801. DOI: 10.1089/thy.2019.0462
https://doi.org/10.1089/thy.2019.0462...
). We considered the studies using the two latter methods as having poorly defined criteria. Two studies (3131 Dode MAS de O, Santos IS. Validade do auto-relato de diabete mellitus gestacional no pós-parto imediato. Cad Saúde Pública. 2009;25(2):251-8. DOI: 10.1590/S0102-311X2009000200003
https://doi.org/10.1590/S0102-311X200900...
,3434 Nunes RD, Flôres ME, Seemann M, Traebert E, Traebert J. Two criteria of oral glucose tolerance test to diagnose gestational diabetes mellitus. Rev Assoc Med Bras. 2020;66(2):139-45. DOI: 10.1590/1806-9282.66.2.139
https://doi.org/10.1590/1806-9282.66.2.1...
) compared different criteria and provided data for both. The characteristics of the included studies and the methods they used to identify GDM are shown in Table 1.
Of the 10 studies based on primary data and measurement of laboratory tests, nine used a universal approach to identify GDM, and one used a two-step approach for this purpose. In the universal approach, the diagnostic test is applied to all study participants, while in the two-step approach, the diagnostic test is applied only to those with a positive result in the first test. Among the studies using the universal approach, most (six) used the IADPSG criteria, two used the 1999 WHO criteria, and one used Carpenter-Coustan values. Studies adopting a two-step approach used FPG or a 50-g glucose challenge as the first test. Finally, we included one study that used the 1999 WHO criteria and the presence of impaired FPG.
Although the report of GDM prevalence was not the primary aim of most studies, they all provided the values (numerators and denominators) required for the calculation of prevalence. The sample size varied widely, from 120 to 79,368 participants, with a median of 792, resulting in the inclusion of 122,635 women in the systematic review. Two studies were conducted at a national level (3232 Souza CM, Malta DC, Iser BPM. Diabetes gestacional autorreferido – uma análise da Pesquisa Nacional de Saúde. Cad Saúde Coletiva. 2022; in press.,3333 Brandao T, Padilha P de C, Nogueira da Gama SG, Leal M do C, Pimenta da Silva Araujo RG, de Barros DC, et al. Gestational weight gain and adverse maternal outcomes in Brazilian women according to body mass index categories: An analysis of data from the Birth in Brazil survey. Clin Nutr ESPEN. 2020;37:114-20. DOI: 10.1016/j.clnesp.2020.03.009
https://doi.org/10.1016/j.clnesp.2020.03...
), while two were conducted in six capitals (88 Schmidt MI, Duncan BB, Reichelt AJ, Branchtein L, Matos MC, Costa e Forti A, et al. Gestational diabetes mellitus diagnosed with a 2-h 75-g oral glucose tolerance test and adverse pregnancy outcomes. Diabetes Care. United States; 2001;24(7):1151-5. DOI: 10.2337/diacare.24.7.1151
https://doi.org/10.2337/diacare.24.7.115...
,2121 Trujillo J, Vigo A, Reichelt A, Duncan BB, Schmidt MI. Fasting plasma glucose to avoid a full OGTT in the diagnosis of gestational diabetes. Diabetes Res Clin Pract. Ireland; 2014;105(3):322-6. DOI: 10.1016/j.diabres.2014.06.001
https://doi.org/10.1016/j.diabres.2014.0...
) and one in five capitals (2020 Nicolosi BF, Souza RT, Mayrink J, Feitosa FE, Rocha Filho EA, Leite DF, et al. Incidence and risk factors for hyperglycemia in pregnancy among nulliparous women: A Brazilian multicenter cohort study. PLoS One. 2020;15(5):e0232664. DOI: 10.1371/journal.pone.0232664
https://doi.org/10.1371/journal.pone.023...
). Ten studies originated in the South and Southeast regions of Brazil.
Quality of the studies
Table 2 summarizes the risk of bias in each study. We categorized the studies according to their overall risk of bias, considering six studies as having a low risk, 13 as having a moderate risk, and two as having a high risk. We considered a high risk of bias when the method used to identify GDM was invalid or when three or more items in the study were considered potentially biased.
Forest plots
The meta-analysis included 16,379 pregnant women. We grouped the studies according to the diagnostic criteria they used to identify GDM and the participants’ age (i.e., whether the study included pregnant women of all ages or just adults aged ≥ 18 years). Studies with primary data and laboratory measurements including only adult women and adopting the IADPSG criteria (n = 3) had a pooled GDM prevalence of 18.0% (95% CI: 16.0-20.1%) and 6,243 participants (Figure 2). This estimate was not heterogenous (I2 = 0%, p = 0.62) and was comparable to that found in studies using the IADPSG criteria based on medical records (18.3%).
For studies based on medical records (n = 5) and using other diagnostic criteria, the overall estimates were 4.3-9.1%, depending on the age of the participants and diagnostic criteria used. Estimates of prevalences in studies using self-reported GDM (n = 3), which included 10,136 participants of all ages, were even lower, with a pooled prevalence of 2.1% (95% CI: 1.5-5.2%). For this pooled estimate, we found significant heterogeneity (I2 = 85.0%, p < 0.01) when we summarized the GDM prevalence. As expected, studies that included women of all ages had a lower prevalence of GDM due to the lower prevalence of this condition among adolescents.
DISCUSSION
The prevalence of GDM in Brazil varied widely according to the diagnostic criteria adopted in the study, with the highest prevalence found in studies using the IADPSG criteria (18.0%, 95% CI: 16.0-20.1%). Because of the heterogeneity across studies, we were unable to provide a pooled estimated prevalence of GDM in Brazil, except in studies using the IADPSG criteria and in those based on self-report. The multitude of diagnostic criteria that we described illustrates the lack of consensus in establishing the diagnosis of this condition over time. Notably, most studies originated in the Southeast and South regions of the country, which have easier access to health care facilities and more research centers.
To the best of our knowledge, this is the first study determining the prevalence of GDM in Brazil using a systematic review and meta-analysis. The variation in prevalence rates is similar to that seen in the literature, with the IADPSG criteria accounting for an almost two times higher proportion of diabetes in pregnancy (4040 Souza CM, Iser BPM. Gestational diabetes mellitus according to different diagnostic criteria: Prevalence and related factors. Midwifery. 2022;113:103428. DOI: 10.1016/j.midw.2022.103428
https://doi.org/10.1016/j.midw.2022.1034...
,4141 Trujillo J, Vigo A, Duncan BB, Falavigna M, Wendland EM, Campos MA, et al. Impact of the International Association of Diabetes and Pregnancy Study Groups criteria for gestational diabetes. Diabetes Res Clin Pract. Ireland; 2015;108(2):288-95. DOI: 10.1016/j.diabres.2015.02.007
https://doi.org/10.1016/j.diabres.2015.0...
). Of note, the IADPSG criteria have been adopted more recently in Brazilian studies, so the higher prevalence associated with its use can be influenced or inflated by the increasing occurrence and diagnosis of GDM in Brazil, following the increasing trend of overall diabetes in the country, as seen worldwide (4242 Reis RCP dos, Duncan BB, Malta DC, Iser BPM, Schmidt MI. Evolution of diabetes in Brazil: prevalence data from the 2013 and 2019 Brazilian National Health Survey. Cad Saúde Pública. 2022;38(Suppl 1):e00149321. DOI: 10.1590/0102-311x00149321
https://doi.org/10.1590/0102-311x0014932...
,4343 International Diabetes Federation. IDF Diabetes Atlas. 10th ed. Brussels: IDF; 2021.). However, when we considered only studies using the IADPSG criteria, we could not find a trend of increasing GDM prevalence over the years.
Our findings are consistent with results from systematic reviews conducted in other countries, which showed that the highest prevalence of GDM occurred in studies using the IADPSG criteria (4444 Saeedi M, Cao Y, Fadl H, Gustafson H, Simmons D. Increasing prevalence of gestational diabetes mellitus when implementing the IADPSG criteria: A systematic review and meta-analysis. Diabetes Research and Clinical Practice. 2021;172:108642. DOI: 10.1016/j.diabres.2020.108642
https://doi.org/10.1016/j.diabres.2020.1...
). According to data from the International Diabetes Federation, the global prevalence of hyperglycemia in pregnancy is 16.7%, of which 80.7% is due to GDM, with similar results in Central and South Latin America, where one out of six live births are affected by hyperglycemia in pregnancy. In our systematic review of Brazilian studies, the prevalence was similar (14.5%) when we analyzed studies using universal screening based on IADPSG thresholds. A global systematic review (22 Behboudi-Gandevani S, Amiri M, Bidhendi Yarandi R, Ramezani Tehrani F. The impact of diagnostic criteria for gestational diabetes on its prevalence: a systematic review and meta-analysis. Diabetol Metab Syndr. 2019;11(1):11. DOI: 10.1186/s13098-019-0406-1
https://doi.org/10.1186/s13098-019-0406-...
) evaluating the impact of diagnostic criteria on the prevalence of GDM had shown that, regardless of the type of screening criteria, the overall prevalence was 4.4% and increased to 10.6% when the IADPSG criteria were used.
Variations in prevalence rates depending on the criteria used for diagnosis of GDM have been previously reported (4040 Souza CM, Iser BPM. Gestational diabetes mellitus according to different diagnostic criteria: Prevalence and related factors. Midwifery. 2022;113:103428. DOI: 10.1016/j.midw.2022.103428
https://doi.org/10.1016/j.midw.2022.1034...
,4444 Saeedi M, Cao Y, Fadl H, Gustafson H, Simmons D. Increasing prevalence of gestational diabetes mellitus when implementing the IADPSG criteria: A systematic review and meta-analysis. Diabetes Research and Clinical Practice. 2021;172:108642. DOI: 10.1016/j.diabres.2020.108642
https://doi.org/10.1016/j.diabres.2020.1...
,4545 Reichelt AJ, Weinert LS, Mastella LS, Gnielka V, Campos MA, Hirakata VN, et al. Clinical characteristics of women with gestational diabetes – comparison of two cohorts enrolled 20 years apart in southern Brazil. São Paulo Med J. 2017;135(4):376-82. DOI: 10.1590/1516-3180.2016.0332190317
https://doi.org/10.1590/1516-3180.2016.0...
). For example, in Europe, an overall 5.4% (95% CI: 3.8-7.8%) prevalence of GDM has been reported, ranging from 6.4% (95% CI: 3.8-10.4%) to 4.7% (95% CI: 2.7-8.1%) when using, respectively, one-step or two-step screening (33 Eades CE, Cameron DM, Evans JMM. Prevalence of gestational diabetes mellitus in Europe: A meta-analysis. Diabetes Res Clin Pract. 2017;129:173-81. DOI: 10.1016/j.diabres.2017.03.030
https://doi.org/10.1016/j.diabres.2017.0...
). Another European study (4646 Paulo MS, Abdo NM, Bettencourt-Silva R, Al-Rifai RH. Gestational diabetes mellitus in Europe: a systematic review and meta-analysis of prevalence studies. Front Endocrinol. 2021;12:691033. DOI: 10.3389/fendo.2021.691033
https://doi.org/10.3389/fendo.2021.69103...
) that analyzed the prevalence of GDM between 2014 and 2019 across 24 European countries reported an overall weighted prevalence of 10.9% (95% CI: 10.0-11.8%, I2 = 100%).
In the Eastern Mediterranean region (4747 Badakhsh M, Daneshi F, Abavisani M, Rafiemanesh H, Bouya S, Sheyback M, et al. Prevalence of gestational diabetes mellitus in Eastern Mediterranean region: a systematic review and meta-analysis. Endocrine. 2019;65(3):505-14. DOI: 10.1007/s12020-019-02026-4
https://doi.org/10.1007/s12020-019-02026...
), the prevalence of GDM has been estimated at 11.7% (95% CI: 10.7-12.6%; I2 = 99.6%) and varied widely depending on the five adopted criteria, suggesting little agreement between the IADPSG (28.2%), Carpenter-Coustan (6.2%), WHO (15.2%), ADA (10.3%), and NDDG (8.1%) criteria. In studies from Africa published from 2013 to 2018 (44 Muche AA, Olayemi OO, Gete YK. Prevalence and determinants of gestational diabetes mellitus in Africa based on the updated international diagnostic criteria: a systematic review and meta-analysis. Arch Public Health. 2019;77(1):36. DOI: 10.1186/s13690-019-0362-0
https://doi.org/10.1186/s13690-019-0362-...
), the random effect pooled prevalence estimate of GDM was 13.6% (95% CI: 10.9-16.2%; I2 = 96.1%), with variations across subregions.
Additional considerations regarding the findings on GDM prevalence in Brazil are worth mentioning. First, we found the lowest prevalence in studies based on a prior self-reported diagnosis of GDM. This result was not surprising since a self-report diagnosis depends on the women's perception of their health status and related factors (4848 Fontanelli M de M, Teixeira JA, Sales CH, Castro MA de, Cesar CLG, Alves MCGP, et al. Validation of self-reported diabetes in a representative sample of São Paulo city. Rev Saúde Pública. 2017;51:20. DOI: 10.1590/s1518-8787.2017051006378
https://doi.org/10.1590/s1518-8787.20170...
,4949 Goldman N. Evaluating the quality of self-reports of hypertension and diabetes. J Clin Epidemiol. 2003;56(2):148-54. DOI: 10.1016/S0895-4356(02)00580-2
https://doi.org/10.1016/S0895-4356(02)00...
), including the degree of use of health care services. For example, the 2013 National Health Survey data reported a low (59%) sensitivity for self-reported diabetes, indicating a high proportion of false-negative results and a likely underestimation in prevalence rates based on self-reporting (5050 Pinheiro PC, Barros MB de A, Szwarcwald CL, Machado ÍE, Malta DC. Diferenças entre medidas autorreferidas e laboratoriais de diabetes, doença renal crônica e hipercolesterolemia. Ciênc Saúde Coletiva. 2021;26(4):1207-19. DOI: 10.1590/1413-81232021264.44582020
https://doi.org/10.1590/1413-81232021264...
). Interestingly, self-reported GDM in the immediate postpartum has great sensitivity (>70%) (3131 Dode MAS de O, Santos IS. Validade do auto-relato de diabete mellitus gestacional no pós-parto imediato. Cad Saúde Pública. 2009;25(2):251-8. DOI: 10.1590/S0102-311X2009000200003
https://doi.org/10.1590/S0102-311X200900...
), with a reported prevalence of 4.1% (95% CI: 3.0-5.5%) compared with 4.3% (95% CI: 3.2-5.7%) for diagnoses based on prenatal cards. Second, the prevalence of GDM based on prenatal care data, even considering possible quality issues, is likely to represent proper population estimates, given the high coverage of prenatal care in Brazil (98.5%) and the fact that more than 80% of the women reportedly undergo at least one measurement of blood glucose level, according to the Birth in Brazil study (5151 Leal M do C, Esteves-Pereira AP, Viellas EF, Domingues RMSM, Gama SGN da. Prenatal care in the Brazilian public health services. Rev Saúde Pública. 2020;54:8. DOI: 10.11606/s1518-8787.2020054001458
https://doi.org/10.11606/s1518-8787.2020...
).
We must consider a few limitations in our study. First, we could not describe the prevalence rates according to some characteristics of the participants, like race or nutritional status (higher BMI), which are known to affect the prevalence of GDM in Brazil (4545 Reichelt AJ, Weinert LS, Mastella LS, Gnielka V, Campos MA, Hirakata VN, et al. Clinical characteristics of women with gestational diabetes – comparison of two cohorts enrolled 20 years apart in southern Brazil. São Paulo Med J. 2017;135(4):376-82. DOI: 10.1590/1516-3180.2016.0332190317
https://doi.org/10.1590/1516-3180.2016.0...
) and worldwide (33 Eades CE, Cameron DM, Evans JMM. Prevalence of gestational diabetes mellitus in Europe: A meta-analysis. Diabetes Res Clin Pract. 2017;129:173-81. DOI: 10.1016/j.diabres.2017.03.030
https://doi.org/10.1016/j.diabres.2017.0...
,44 Muche AA, Olayemi OO, Gete YK. Prevalence and determinants of gestational diabetes mellitus in Africa based on the updated international diagnostic criteria: a systematic review and meta-analysis. Arch Public Health. 2019;77(1):36. DOI: 10.1186/s13690-019-0362-0
https://doi.org/10.1186/s13690-019-0362-...
,4747 Badakhsh M, Daneshi F, Abavisani M, Rafiemanesh H, Bouya S, Sheyback M, et al. Prevalence of gestational diabetes mellitus in Eastern Mediterranean region: a systematic review and meta-analysis. Endocrine. 2019;65(3):505-14. DOI: 10.1007/s12020-019-02026-4
https://doi.org/10.1007/s12020-019-02026...
). Most studies did not report maternal age or BMI, limiting the possibility of adjusted analysis. Additionally, we were unable to perform subgroup analysis by Brazilian macro-regions since most of the included studies were specific to one center or region. Finally, the different settings across studies limited our ability to provide a pooled prevalence estimate. However, the heterogeneity between studies reflecting the status of GDM in Brazil over time is, by itself, an important finding of our study.
In conclusion, the diagnostic criteria of GDM varied substantially, which is the main reason for discrepancies in this condition's prevalence. The pooled prevalence was greater when we considered studies adopting the IADPSG criteria based on primary laboratory data (18.0%, 95% CI: 16.0-20.1%), followed by the use of medical records (range 4.3-9.1%) and self-reported data (2.1%, 95% CI: 1.5-5.2%). Other factors also contributed to the variation in GDM prevalence. For example, reports that included only adult women had higher prevalences than those that also included adolescents. In addition, referral centers, by having higher proportions of high-risk pregnancies, had a higher prevalence of GDM. Although global uniform criteria for GDM screening and diagnosis have been desired for a long time and will allow simplification of the guidelines and more adequate international comparisons, we have not reached this stage yet. New studies in the field may help reach this goal.
-
Funding: Funding for this review was provided by the Ministry of Health (TED 95/2019) and the LINDA Brasil Study (Fundação Médica do Rio Grande do Sul).
-
Ethics approval and consent to participate: not applicable.
Availability of data and materials
all data pertaining to this study are contained and presented in this document. Additional data may be available upon request.
REFERENCES
-
1Ye W, Luo C, Huang J, Li C, Liu Z, Liu F. Gestational diabetes mellitus and adverse pregnancy outcomes: systematic review and meta-analysis. BMJ. 2022;377:e067946. DOI: 10.1136/bmj-2021-067946
» https://doi.org/10.1136/bmj-2021-067946 -
2Behboudi-Gandevani S, Amiri M, Bidhendi Yarandi R, Ramezani Tehrani F. The impact of diagnostic criteria for gestational diabetes on its prevalence: a systematic review and meta-analysis. Diabetol Metab Syndr. 2019;11(1):11. DOI: 10.1186/s13098-019-0406-1
» https://doi.org/10.1186/s13098-019-0406-1 -
3Eades CE, Cameron DM, Evans JMM. Prevalence of gestational diabetes mellitus in Europe: A meta-analysis. Diabetes Res Clin Pract. 2017;129:173-81. DOI: 10.1016/j.diabres.2017.03.030
» https://doi.org/10.1016/j.diabres.2017.03.030 -
4Muche AA, Olayemi OO, Gete YK. Prevalence and determinants of gestational diabetes mellitus in Africa based on the updated international diagnostic criteria: a systematic review and meta-analysis. Arch Public Health. 2019;77(1):36. DOI: 10.1186/s13690-019-0362-0
» https://doi.org/10.1186/s13690-019-0362-0 -
5O'Sullivan JB. Establishing criteria for gestational diabetes. Diabetes Care. 1980;3(3):437-9. DOI: 10.2337/diacare.3.3.437
» https://doi.org/10.2337/diacare.3.3.437 -
6National Diabetes Data Group. Classification and diagnosis of diabetes mellitus and other categories of glucose intolerance. Diabetes. 1979;28(12):1039-57. DOI: 10.2337/diab.28.12.1039
» https://doi.org/10.2337/diab.28.12.1039 -
7World Health Organization. WHO Expert Committee on Diabetes Mellitus [meeting held in Geneva from 25 September to 1 October 1979]: second report. Geneva: WHO; 1980.
-
8Schmidt MI, Duncan BB, Reichelt AJ, Branchtein L, Matos MC, Costa e Forti A, et al. Gestational diabetes mellitus diagnosed with a 2-h 75-g oral glucose tolerance test and adverse pregnancy outcomes. Diabetes Care. United States; 2001;24(7):1151-5. DOI: 10.2337/diacare.24.7.1151
» https://doi.org/10.2337/diacare.24.7.1151 -
9Schmidt MI, Reichelt AJ. Consenso sobre diabetes gestacional e diabetes pré-gestacional. Arq Bras Endocrinol Metab. 1999;43(1):14-20. DOI: 10.1590/S0004-27301999000100005
» https://doi.org/10.1590/S0004-27301999000100005 -
10The Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Diabetes Care. 1997;20(7):1183-97. DOI: 10.2337/diacare.20.7.1183
» https://doi.org/10.2337/diacare.20.7.1183 -
11The HAPO Study Cooperative Research Group. Hyperglycemia and adverse pregnancy outcomes. N Engl J Med. 2008;358(19):1991-2002. DOI: 10.1056/NEJMoa0707943
» https://doi.org/10.1056/NEJMoa0707943 -
12International Association of Diabetes and Pregnancy Study Groups Consensus Panel. International Association of Diabetes and Pregnancy Study Groups recommendations on the diagnosis and classification of hyperglycemia in pregnancy. Diabetes Care. 2010;33(3):676-82. DOI: 10.2337/dc09-1848
» https://doi.org/10.2337/dc09-1848 -
13Hod M, Kapur A, Sacks DA, Hadar E, Agarwal M, Di Renzo GC, et al. The International Federation of Gynecology and Obstetrics (FIGO) Initiative on gestational diabetes mellitus: A pragmatic guide for diagnosis, management, and care. Int J Gynaecol Obstet. 2015;131 Suppl 3:S173-211. DOI: 10.1016/S0020-7292(15)30033-3
» https://doi.org/10.1016/S0020-7292(15)30033-3 -
14American Diabetes Association. Standards of medical care in diabetes—2010. Diabetes Care. 2010;33(Supplement_1):S11-61. DOI: 10.2337/dc10-S011
» https://doi.org/10.2337/dc10-S011 -
15World Health Organization. Diagnostic criteria and classification of hyperglycaemia first detected in pregnancy. Geneva: WHO; 2013.
-
16National Institute for Health and Care Excellence. Diabetes in pregnancy: management from preconception to the postnatal period. London: NICE; 2020.
-
17ElSayed NA, Aleppo G, Aroda VR, Bannuru RR, Brown FM, Bruemmer D, et al. 2. Classification and Diagnosis of Diabetes: Standards of Care in Diabetes—2023. Diabetes Care. 2023;46(Supplement_1):S19-40. DOI: 10.2337/dc23-S002
» https://doi.org/10.2337/dc23-S002 -
18Organização Pan-Americana da Saúde. Rastreamento e diagnóstico de diabetes mellitus gestacional no Brasil. Brasília: OPAS; 2017.
-
19Hoy D, Brooks P, Woolf A, Blyth F, March L, Bain C, et al. Assessing risk of bias in prevalence studies: modification of an existing tool and evidence of interrater agreement. J Clin Epidemiol. 2012;65(9):934-9. DOI: 10.1016/j.jclinepi.2011.11.014
» https://doi.org/10.1016/j.jclinepi.2011.11.014 -
20Nicolosi BF, Souza RT, Mayrink J, Feitosa FE, Rocha Filho EA, Leite DF, et al. Incidence and risk factors for hyperglycemia in pregnancy among nulliparous women: A Brazilian multicenter cohort study. PLoS One. 2020;15(5):e0232664. DOI: 10.1371/journal.pone.0232664
» https://doi.org/10.1371/journal.pone.0232664 -
21Trujillo J, Vigo A, Reichelt A, Duncan BB, Schmidt MI. Fasting plasma glucose to avoid a full OGTT in the diagnosis of gestational diabetes. Diabetes Res Clin Pract. Ireland; 2014;105(3):322-6. DOI: 10.1016/j.diabres.2014.06.001
» https://doi.org/10.1016/j.diabres.2014.06.001 -
22Vernini JM, Nicolosi BF, Arantes MA, Costa RA, Magalhães CG, Corrente JE, et al. Metabolic syndrome markers and risk of hyperglycemia in pregnancy: a cross-sectional cohort study. Sci Rep. 2020;10(1):21042. DOI: 10.1038/s41598-020-78099-3
» https://doi.org/10.1038/s41598-020-78099-3 -
23Santos EMF, Amorim LP de, Costa OLN, Oliveira N, Guimarães AC. Perfil de risco gestacional e metabólico no serviço de pré-natal de maternidade pública do Nordeste do Brasil. Rev Bras Ginecol Obstet. 2012;34(3):102-6. DOI: 10.1590/S0100-72032012000300002
» https://doi.org/10.1590/S0100-72032012000300002 -
24Ayach W, Costa RAA, Calderon I de MP, Rudge MVC. Comparison between 100-g glucose tolerance test and two other screening tests for gestational diabetes: combined fasting glucose with risk factors and 50-g glucose tolerance test. Sao Paulo Med J. Brazil; 2006;124(1):4-9. DOI: 10.1590/s1516-31802006000100002
» https://doi.org/10.1590/s1516-31802006000100002 -
25Barbieiri P, Nunes JC, Torres AG, Nishimura RY, Zuccolotto DCC, Crivellenti LC, et al. Indices of dietary fat quality during midpregnancy is associated with gestational diabetes. Nutrition. United States; 2016;32(6):656-61. DOI: 10.1016/j.nut.2015.12.002
» https://doi.org/10.1016/j.nut.2015.12.002 -
26Nascimento GR, Alves LV, Leal Fonseca C, Natal Figueiroa J, Alves JG. Dietary patterns and gestational diabetes mellitus in a low income pregnant women population in Brazil - a cohort study. Arch Latinoam Nutr. 2016;66(4):301-8.
-
27Valladares CG, Komka SB. Prevalência de diabetes mellitus gestacional em gestantes de um centro de saúde de Brasília - DF. Comun Ciênc Saúde. 2008;19(1):11-7.
-
28Alves JG, Souza ASR, Figueiroa JN, de Araújo CAL, Guimarães A, Ray JG. Visceral adipose tissue depth in early pregnancy and gestational diabetes mellitus - a cohort study. Sci Rep. 2020;10(1):2032. DOI: 10.1038/s41598-020-59065-5
» https://doi.org/10.1038/s41598-020-59065-5 -
29Dode MAS de O, Santos I da S dos. Fatores de risco para diabetes mellitus gestacional na coorte de nascimentos de Pelotas, Rio Grande do Sul, Brasil, 2004. Cad Saúde Pública. 2009;25(5):1141-52. DOI: 10.1590/S0102-311X2009000500021
» https://doi.org/10.1590/S0102-311X2009000500021 -
30Lima RJCP, Batista RFL, Ribeiro MRC, Ribeiro CCC, Simões VMF, Neto PML, et al. Prepregnancy body mass index, gestational weight gain, and birth weight in the BRISA cohort. Rev Saude Publica. 2018;52:46-46. DOI: 10.11606/S1518-8787.2018052000125
» https://doi.org/10.11606/S1518-8787.2018052000125 -
31Dode MAS de O, Santos IS. Validade do auto-relato de diabete mellitus gestacional no pós-parto imediato. Cad Saúde Pública. 2009;25(2):251-8. DOI: 10.1590/S0102-311X2009000200003
» https://doi.org/10.1590/S0102-311X2009000200003 -
32Souza CM, Malta DC, Iser BPM. Diabetes gestacional autorreferido – uma análise da Pesquisa Nacional de Saúde. Cad Saúde Coletiva. 2022; in press.
-
33Brandao T, Padilha P de C, Nogueira da Gama SG, Leal M do C, Pimenta da Silva Araujo RG, de Barros DC, et al. Gestational weight gain and adverse maternal outcomes in Brazilian women according to body mass index categories: An analysis of data from the Birth in Brazil survey. Clin Nutr ESPEN. 2020;37:114-20. DOI: 10.1016/j.clnesp.2020.03.009
» https://doi.org/10.1016/j.clnesp.2020.03.009 -
34Nunes RD, Flôres ME, Seemann M, Traebert E, Traebert J. Two criteria of oral glucose tolerance test to diagnose gestational diabetes mellitus. Rev Assoc Med Bras. 2020;66(2):139-45. DOI: 10.1590/1806-9282.66.2.139
» https://doi.org/10.1590/1806-9282.66.2.139 -
35Santos PA dos, Madi JM, Silva ER da, Vergani D de OP, Araújo BF de, Garcia RMR. Diabetes gestacional na população atendida pelo sistema público de saúde no Brasil. Prevalência e fatores de risco. Rev Bras Ginecol Obstet. 2020;42(1):12-8. DOI: 10.1055/s-0039-1700797
» https://doi.org/10.1055/s-0039-1700797 -
36Zapelini RM, Martinelli MT, João RM, Iser BPM. Critérios diagnósticos e prevalência de Diabetes Mellitus Gestacional em um hospital do sul de Santa Catarina. Rev AMRIGS. 2015;59(3):177-81.
-
37Oliveira ACM de, Graciliano NG. Síndrome hipertensiva da gravidez e diabetes mellitus gestacional em uma maternidade pública de uma capital do Nordeste brasileiro, 2013: prevalência e fatores associados. Epidemiol Serv Saúde. 2015;24(3):441-51. DOI: 10.5123/S1679-49742015000300010
» https://doi.org/10.5123/S1679-49742015000300010 -
38Teixeira CR de S, Franco LJ, Monteiro RA, Granado F. Diabetes nos partos hospitalares em sistemas de saúde público e privado. Rev Saúde Pública. 2013;47(3):460-9. DOI: 10.1590/s0034-8910.2013047003687
» https://doi.org/10.1590/s0034-8910.2013047003687 -
39Silva de Morais N, Ayres Saraiva D, Corcino C, Berbara T, Schtscherbyna A, Moreira K, et al. Consequences of Iodine Deficiency and Excess in Pregnancy and Neonatal Outcomes: A Prospective Cohort Study in Rio de Janeiro, Brazil. Thyroid. United States; 2020;30(12):1792-801. DOI: 10.1089/thy.2019.0462
» https://doi.org/10.1089/thy.2019.0462 -
40Souza CM, Iser BPM. Gestational diabetes mellitus according to different diagnostic criteria: Prevalence and related factors. Midwifery. 2022;113:103428. DOI: 10.1016/j.midw.2022.103428
» https://doi.org/10.1016/j.midw.2022.103428 -
41Trujillo J, Vigo A, Duncan BB, Falavigna M, Wendland EM, Campos MA, et al. Impact of the International Association of Diabetes and Pregnancy Study Groups criteria for gestational diabetes. Diabetes Res Clin Pract. Ireland; 2015;108(2):288-95. DOI: 10.1016/j.diabres.2015.02.007
» https://doi.org/10.1016/j.diabres.2015.02.007 -
42Reis RCP dos, Duncan BB, Malta DC, Iser BPM, Schmidt MI. Evolution of diabetes in Brazil: prevalence data from the 2013 and 2019 Brazilian National Health Survey. Cad Saúde Pública. 2022;38(Suppl 1):e00149321. DOI: 10.1590/0102-311x00149321
» https://doi.org/10.1590/0102-311x00149321 -
43International Diabetes Federation. IDF Diabetes Atlas. 10th ed. Brussels: IDF; 2021.
-
44Saeedi M, Cao Y, Fadl H, Gustafson H, Simmons D. Increasing prevalence of gestational diabetes mellitus when implementing the IADPSG criteria: A systematic review and meta-analysis. Diabetes Research and Clinical Practice. 2021;172:108642. DOI: 10.1016/j.diabres.2020.108642
» https://doi.org/10.1016/j.diabres.2020.108642 -
45Reichelt AJ, Weinert LS, Mastella LS, Gnielka V, Campos MA, Hirakata VN, et al. Clinical characteristics of women with gestational diabetes – comparison of two cohorts enrolled 20 years apart in southern Brazil. São Paulo Med J. 2017;135(4):376-82. DOI: 10.1590/1516-3180.2016.0332190317
» https://doi.org/10.1590/1516-3180.2016.0332190317 -
46Paulo MS, Abdo NM, Bettencourt-Silva R, Al-Rifai RH. Gestational diabetes mellitus in Europe: a systematic review and meta-analysis of prevalence studies. Front Endocrinol. 2021;12:691033. DOI: 10.3389/fendo.2021.691033
» https://doi.org/10.3389/fendo.2021.691033 -
47Badakhsh M, Daneshi F, Abavisani M, Rafiemanesh H, Bouya S, Sheyback M, et al. Prevalence of gestational diabetes mellitus in Eastern Mediterranean region: a systematic review and meta-analysis. Endocrine. 2019;65(3):505-14. DOI: 10.1007/s12020-019-02026-4
» https://doi.org/10.1007/s12020-019-02026-4 -
48Fontanelli M de M, Teixeira JA, Sales CH, Castro MA de, Cesar CLG, Alves MCGP, et al. Validation of self-reported diabetes in a representative sample of São Paulo city. Rev Saúde Pública. 2017;51:20. DOI: 10.1590/s1518-8787.2017051006378
» https://doi.org/10.1590/s1518-8787.2017051006378 -
49Goldman N. Evaluating the quality of self-reports of hypertension and diabetes. J Clin Epidemiol. 2003;56(2):148-54. DOI: 10.1016/S0895-4356(02)00580-2
» https://doi.org/10.1016/S0895-4356(02)00580-2 -
50Pinheiro PC, Barros MB de A, Szwarcwald CL, Machado ÍE, Malta DC. Diferenças entre medidas autorreferidas e laboratoriais de diabetes, doença renal crônica e hipercolesterolemia. Ciênc Saúde Coletiva. 2021;26(4):1207-19. DOI: 10.1590/1413-81232021264.44582020
» https://doi.org/10.1590/1413-81232021264.44582020 -
51Leal M do C, Esteves-Pereira AP, Viellas EF, Domingues RMSM, Gama SGN da. Prenatal care in the Brazilian public health services. Rev Saúde Pública. 2020;54:8. DOI: 10.11606/s1518-8787.2020054001458
» https://doi.org/10.11606/s1518-8787.2020054001458
SUPPLEMENTARY
Publication Dates
-
Publication in this collection
27 Oct 2023 -
Date of issue
2023
History
-
Received
22 Dec 2022 -
Accepted
17 July 2023